An object of the present invention is to provide magnesium oxide for an annealing separator which is useful for obtaining grain-oriented electromagnetic steel sheets with excellent magnetic properties and insulating properties. To resolve the above object, an aspect of the present invention resides in magnesium oxide for an annealing separator having a sulfur content of 0.1 to 0.5 mass % and an aggregation degree R.sub.Blaine/R.sub.BET of 3.0 to 5.5 wherein R.sub.Blaine is the particle size calculated from the Blaine specific surface area and R.sub.BET is the particle size calculated from the BET specific surface area.

There are provided a new type of crystal laminate of an alkaline earth metal titanate having improved catalytic activity, and a method for producing the same. The crystal laminate is provided having a crystal of the alkaline earth metal titanate as a constitutional unit, wherein the crystal being the constitutional unit is a cubic crystal, a tetragonal crystal or an orthorhombic crystal; the crystal being the constitutional unit has a primary particle diameter of 500 nm or less; and the crystal is layered with an orientation in a {100} plane direction thereof.

The invention relates to Chevrel-phase materials and methods of preparing these materials utilizing a precursor approach. The Chevrel-phase materials are useful in assembling electrodes, e.g., cathodes, for use in electrochemical cells, such as rechargeable batteries. The Chevrel-phase materials have a general formula of Mo.sub.6Z.sub.8 (Z=sulfur) or Mo.sub.6Z.sup.1.sub.8-yZ.sup.2.sub.y (Z.sup.1=sulfur; Z.sup.2=selenium), and partially cuprated Cu.sub.1Mo.sub.6S.sub.8 as well as partially de-cuprated Cu.sub.1-xMg.sub.xMo.sub.6S.sub.8 and the precursors have a general formula of M.sub.xMo.sub.6Z.sub.8 or M.sub.xMo.sub.6Z.sup.1.sub.8-yZ.sup.2.sub.y, M=Cu. The cathode containing the Chevrel-phase material in accordance with the invention can be combined with a magnesium-containing anode and an electrolyte.

The present invention provides alumina hydrate particles, a flame retardant and a resin composition that are each for an electric wire/cable covering material improvable in flame retardancy and mechanical properties while the covering material keeps acid resistance; such an electric wire/cable; and producing methods thereof. The alumina hydrate particles of the present invention for electric wire/cable covering material have an average particle size of 0.5 to 2.5 μm, and having a primary particle variation R of 24% or less, the variation R being represented by the following expression:
primary particle variation R (%)=“standard deviationσ(μm) of major axis diameters of the primary particles”/“average value(μm) of the major axis diameters of the primary particles”×100.

A method includes positioning a porous structure in a pressure cell; injecting an inert pressure medium within the pressure cell; and pressurizing the pressure cell to a pressure that thermodynamically favors a crystalline phase of the porous structure over an amorphous phase of the porous structure to transition the amorphous phase of the porous structure into the crystalline phase of the porous structure.

Disclosed herein are a nickel oxide fine powder that is suitable as a material for electronic parts and has a controlled sulfur content, a low chlorine content, and a fine particle size and a method for industrially and stably producing such a nickel oxide fine powder.

Nickel hydroxide obtained by neutralizing an aqueous nickel sulfate solution with an alkali is heat-treated in a non-reducing atmosphere at a temperature higher than 650° C. but lower than 1050° C. to form nickel oxide particles, and a sintered compact of nickel oxide particles that may be formed during the heat treatment is pulverized by preferably allowing the nickel oxide particles to collide with one another. The thus obtained nickel oxide fine powder has a sulfur content of 400 mass ppm or less, a chlorine content of 50 mass ppm or less, a sodium content of 100 mass ppm or less, and a specific surface area of 3 m.sup.2/g or more but less than 6 m.sup.2/g.

A process for treating a sulfurous fluid to form gypsum and magnesium carbonate, whereby the sulfurous fluid is scrubbed with a sequestrating agent to yield a scrubbed fluid, gypsum and magnesium sulfate. The flue gas desulfurized gypsum is isolated from the magnesium sulfate solution by filtration or centrifugation. The magnesium sulfate is reacted with a carbonate salt to produce a magnesium carbonate whereby the reaction conditions are controlled to control the properties of the magnesium carbonate produced.

The present invention relates to a method of preparing a hydrophobic metal oxide-silica composite aerogel having a high specific surface area and a low tap density and a hydrophobic metal oxide-silica composite aerogel prepared thereby. Thus, the preparation method may not only have excellent productivity and economic efficiency due to a relatively simpler preparation process and shorter preparation time than the related art, but may also prepare a hydrophobic metal oxide-silica composite aerogel having a high specific surface area and a low tap density.

The present invention relates to a process for the manufacturing of a calcium carbonate-comprising material, a calcium carbonate-comprising material obtained by a process as well as the use of the calcium carbonate-comprising material for paper filler and paper coating applications, cigarette paper applications, for plastics applications or in paints, coatings, adhesives, replacement of titanium dioxide, preferably in paints, sealants, food, feed, pharma, concrete, cement, cosmetic, water treatment and/or agriculture applications.

Powder comprising particles comprising a matrix material and silicon-based domains dispersed in this matrix material, whereby the matrix material is carbon or a material that can be thermally decomposed to carbon, whereby either part of the silicon-based domains are present in the form of agglomerates of silicon-based domains whereby at least 98% of these agglomerates have a maximum size of 3 μm or less, or the silicon-based domains are not at all agglomerated into agglomerates.